To compare two different iron injections for treatment of anaemia in pregnancy

Not Applicable

• Conditions: Health Condition 1: null- Pregnant anaemic women

• Registration Number: CTRI/2017/07/009088
• Lead Sponsor: All India Institute of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 24 November 2021

Recruitment & Eligibility

• Status: Open to Recruitment
• Sex: Not specified
• Target Recruitment: 60

Inclusion Criteria

1)Pregnant women with period of gestation 16-36weeks

2)Iron deficiency anemia with serum Hb >6g/dl and <10g/dl

3)Not tolerating oral iron

4)Non-compliant to oral iron therapy

5)Willing to participate and follow up

Exclusion Criteria

1)Age less than 18 years

2)Anemia due to causes other than iron deficiency anemia

3)Co existing disorders of erythropoiesis or hemochromatosis

4)Chronic infections like hepatitis and HIV

5)Serum transaminase level > 1.5 times the upper limit of normal

6)Serum creatinine level > 2.0mg/dl

7)Patients with history of allergic reaction to intravenous iron infusion

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
1)Change in Hb level from baselineTimepoint: 0,3,6,12 weeks

Secondary Outcome Measures

Name	Time	Method
1)Change in ferritin levels <br/ ><br>2)Number of women achieving normalisation of Hb (â?¥11g/dL) <br/ ><br>3)Change in serum iron and RBC indices <br/ ><br>4)Normalisation of RDW <br/ ><br>5)Change in fatigue levels <br/ ><br>6)Change in well-being score <br/ ><br>7)Safety and side effects of treatment <br/ ><br>8)Obstetrical outcome <br/ ><br>Timepoint: 0,3,6,12 weeks